Reacción #996528

ord-fe06b0af90f045d88051afe5b3b469fd

Disolventes

Condiciones de reacción

Temperatura
110°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe vial was flushed with nitrogen
  2. 2
    Otrosealed with a Teflon-
  3. 3
    Otrolined cap
  4. 4
    Otroplaced in an oil bath
  5. 5
    TemperaturaThe reaction was cooled to ambient temperature
  6. 6
    workup.ADDITIONdiluted with chloroform
  7. 7
    Filtraciónfiltered through a bed of CELITE
  8. 8
    Filtraciónfilter agent
  9. 9
    OtroThe solvent was evaporated
  10. 10
    Otrothe residue was purified by column chromatography on a Biotage Horizon™ High-Performance Flash Chromatography instrument
  11. 11
    OtroThe purification
  12. 12
    Lavadowas carried out eluting with chloroform
  13. 13
    OtroAdditional purification
  14. 14
    Otroby recrystallization from acetonitrile

Procedimiento

7-Bromo-2-ethoxymethyl-1-(3-isopropoxypropyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.75 g), 2(1H)-pyridone (0.20 g), copper(I) iodide (68 mg), N,N′-dimethylethylenediamine (75 μL), potassium phosphate (0.79 g) and dioxane (2.7 mL) were added to a scintillation vial. The vial was flushed with nitrogen, sealed with a Teflon-lined cap, placed in an oil bath, and heated to 110° C. for 60 hours. The reaction was cooled to ambient temperature, diluted with chloroform and filtered through a bed of CELITE filter agent. The solvent was evaporated and the residue was purified by column chromatography on a Biotage Horizon™ High-Performance Flash Chromatography instrument using a silica gel cartridge. The purification was carried out eluting with chloroform:CMA in a gradient from 99:1 to 75:25. Additional purification by recrystallization from acetonitrile provided 0.38 g of 1-[4-amino-2-ethoxymethyl-1-(3-isopropoxypropyl)-1H-imidazo[4,5-c]quinolin-7-yl]-1H-pyridin-2-one as a tan solid, mp 161-163.5° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08017779B2uspto-grants-2011_09